Phenacylamine → 2-Aminoacetophenone 3-chlorophenylhydrazone
反応式
[NH2:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.[Cl:11][C:12]1[CH:13]=[C:14]([NH:18][NH2:19])[CH:15]=[CH:16][CH:17]=1>CC(O)=O.CCO.O>[Cl:11][C:12]1[CH:13]=[C:14]([NH:18][N:19]=[C:3]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:2][NH2:1])[CH:15]=[CH:16][CH:17]=1参加物
6
実験手順
A mixture of 3.12 g 2-aminoacetophenone and 3.29 g 3-chlorophenylhydrazine in 4 ml HOAc and 20 ml EtOH was refluxed for one hour. The cooled reaction mixture was diluted with water and the precipitate was collected, washed with water, and dried to give 5.16 g solid. Recrystallization from methanol gave 2.12 g solid, m.p. 131°-134° C.
後処理
- temperaturewas refluxed for one hour
- customThe cooled reaction mixture
- customthe precipitate was collected
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-f0fb4ee128634fbc8c8d3a1e252fae6f
- 出典データセット
- uspto-grants-1993_05
- 特許番号
- US05214059
反応ノート
読み込み中…